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纤维化间质性肺疾病急性加重期的类固醇治疗。

Steroid therapy in acute exacerbation of fibrotic interstitial lung disease.

机构信息

Department of Respiratory Medicine, Alfred Health, Melbourne, Victoria, Australia.

Department of Respiratory and Sleep Medicine, Eastern Health, Melbourne, Victoria, Australia.

出版信息

Respirology. 2024 Sep;29(9):795-802. doi: 10.1111/resp.14763. Epub 2024 Jun 2.

Abstract

BACKGROUND AND OBJECTIVE

Evidence for the benefit of steroid therapy in acute exacerbations (AEs) of idiopathic pulmonary fibrosis (IPF) is limited; however, they remain a cornerstone of management in other fibrotic interstitial lung diseases. This retrospective observational study assesses the effect of steroid treatment on in-hospital mortality in patients with acute exacerbation of fibrotic interstitial lung disease (AE-FILD) including IPF and non-IPF ILDs.

METHODS

AE-FILD cases over a 10-year period were filtered using a code-based algorithm followed by individual case evaluation. Binary logistic regression analysis was used to assess the relationship between corticosteroid treatment (defined as ≥0.5 mg/kg/day of prednisolone-equivalent for ≥3 days within the first 72 h of admission) and in-hospital mortality or need for lung transplantation. Secondary outcomes included readmission, overall survival, requirement for domiciliary oxygen and rehabilitation.

RESULTS

Across two centres a total of 107 AE-FILD subjects were included, of which 46 patients (43%) received acute steroid treatment. The steroid cohort was of younger age with fewer comorbidities but had higher oxygen requirements. Pre-admission FVC and DLCO, distribution of diagnoses and smoking history were similar. The mean steroid treatment dose was 4.59 mg/kg/day. Steroid use appeared to be associated with increased risk of inpatient mortality or transplantation (OR 4.11; 95% CI 1.00-16.83; p = 0.049). In the steroid group, there appeared to be a reduced risk of all-cause mortality in non-IPF patients (HR 0.21; 95% CI 0.04-0.96; p = 0.04) compared to their IPF counterparts. Median survival was reduced in the steroid group (221 vs. 520.5 days) with increased risk of all-cause mortality (HR 3.25; 95% CI 1.56-6.77; p < 0.01).

CONCLUSION

In this two-centre retrospective study of 107 patients, AE-FILD demonstrates a high risk of mortality, at a level similar to that seen for AE-IPF, despite steroid treatment. Clinicians should consider other precipitating factors for exacerbations and use steroids judiciously. Further prospective trials are needed to determine the role of corticosteroids in AE-FILD.

摘要

背景和目的

类固醇治疗对特发性肺纤维化(IPF)急性加重(AE)的益处证据有限;然而,它们仍然是其他纤维性间质性肺疾病管理的基石。这项回顾性观察研究评估了类固醇治疗对包括 IPF 和非 IPFILD 在内的纤维性间质性肺疾病急性加重(AE-FILD)患者住院死亡率的影响。

方法

使用基于代码的算法筛选了 10 年来的 AE-FILD 病例,然后进行了个体病例评估。使用二元逻辑回归分析评估皮质类固醇治疗(定义为入院前 72 小时内每天≥0.5mg/kg 泼尼松等效剂量≥3 天)与住院死亡率或肺移植的关系。次要结局包括再入院、总生存率、家庭氧疗和康复需求。

结果

在两个中心共纳入了 107 例 AE-FILD 患者,其中 46 例(43%)接受了急性类固醇治疗。类固醇组年龄较小,合并症较少,但氧需求较高。入院前 FVC 和 DLCO、诊断分布和吸烟史相似。平均类固醇治疗剂量为 4.59mg/kg/天。类固醇的使用似乎与住院死亡率或移植风险增加相关(OR 4.11;95%CI 1.00-16.83;p=0.049)。在类固醇组中,与 IPF 患者相比,非 IPF 患者的全因死亡率似乎降低(HR 0.21;95%CI 0.04-0.96;p=0.04)。与非类固醇组相比,类固醇组的中位生存期缩短(221 与 520.5 天),全因死亡率增加(HR 3.25;95%CI 1.56-6.77;p<0.01)。

结论

在这项对 107 例患者的两中心回顾性研究中,AE-FILD 显示出高死亡率风险,与 AE-IPF 相似,尽管进行了类固醇治疗。临床医生应考虑其他加重的诱发因素,并谨慎使用类固醇。需要进一步的前瞻性试验来确定皮质类固醇在 AE-FILD 中的作用。

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